Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability

Published:2014-01-10 Issue:1 Volume:7 Page:
ISSN:1755-8166
Container-title:Molecular Cytogenetics
language:en
Short-container-title:Mol Cytogenet

Author:

Xu Fang,Li Lun,Schulz Vincent P,Gallagher Patrick G,Xiang Bixia,Zhao Hongyu,Li Peining

Publisher

Springer Science and Business Media LLC

Subject

Biochemistry (medical),Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Link

https://link.springer.com/content/pdf/10.1186/1755-8166-7-4.pdf

Reference38 articles.

1. Chelly J, Khelfaoui M, Francis F, Cherif B, Bienvenu T: Genetics and pathophysiology of mental retardation. Eur J Hum Genet 2006, 14: 701–713. 10.1038/sj.ejhg.5201595

2. Shaffer LG: American College of Medical Genetics guideline on the cytogenetic evaluation of the individual with developmental delay or mental retardation. Genet Med 2005, 7: 650–654. 10.1097/01.gim.0000186545.83160.1e

3. Miller DT, Adam MP, Aradhya S, Biesecker LG, Brothman AR, Carter NP, Church DM, Crolla JA, Eichler EE, Epstein CJ, et al.: Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet 2010, 86: 749–764. 10.1016/j.ajhg.2010.04.006

4. Xiang B, Li A, Valentin D, Nowak NJ, Zhao H, Li P: Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay. Am J Med Genet A 2008, 146A: 1942–1954. 10.1002/ajmg.a.32411

5. Hayashi S, Imoto I, Aizu Y, Okamoto N, Mizuno S, Kurosawa K, Honda S, Araki S, Mizutani S, Numabe H, et al.: Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies. J Hum Genet 2010, 56: 110–124.

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Progresses in genetic testing in congenital heart disease;Medicine Plus;2024-06

2. Genetic Databases and Online Ring Chromosome Registry;Human Ring Chromosomes;2024

3. Ring Chromosome 9;Human Ring Chromosomes;2024

4. Historical Perspective of Human Ring Chromosomes;Human Ring Chromosomes;2024

5. 15q26.3 deletions distal to IGF1R cause growth retardation, congenital heart defect and skeletal anomalies: Case report and review of literature;American Journal of Medical Genetics Part A;2023-07-12

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3